Informatics and Computationally Assisted Discovery of Anti-Inflammatory Diterpenoids from Isodon rubescens

20 October 2023, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Diterpenoids occupy a valuable region of the natural products diversity space with wide ranges of bioactivities and complex structures, providing potential applications for the development of therapeutics. Five new abietane-type diterpenoids salvonitin B (1), salvonitin C (2), prionoid G (3), prionidipene F (4), viroxocin B (5), one new totarane-type diterpenoid plebedipene E (6) and one new sempervirane-type diterpenoid hispidanol C (7) were isolated from Isodon rubescens (I. rubescens). Their structures were established by spectroscopic analysis, electronic circular dichroism (ECD) calculations, and X-ray diffraction analysis. In the evaluation of bioactivities, compound 4 (10 μM) increased cell viability (0.872 ± 0.157) in lipopolysaccharide-induced RAW 264.7 cells.

Keywords

Diterpenoids
Isodon

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.